This invention belongs to the field of
biomedical technology, specifically disclosing a nanomicelle FluDox-MIC, its preparation method, and its uses. This nanomicelle is formed by the self-
assembly of flumatinib and
doxorubicin co-loaded in mPEG-DSPE, exhibiting pH-responsive release properties. Upon entering the
tumor microenvironment, it releases the
drug. The released flumatinib induces the degradation of the poliovirus
receptor (PVR / CD155), relieving its inhibitory
signal on NK cells and reactivating innate immune surveillance. Simultaneously, low-
dose doxorubicin induces significant
immunogenic cell death (ICD), initiating and amplifying tumor-specific
T cell-mediated adaptive
immunity. Through the synergistic activation of innate and adaptive
immunity, the nanomicelle of this invention can effectively inhibit
melanoma growth and overcome
immunotherapy resistance, showing promising clinical application prospects.